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rs45502703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45502703(C;C)
Make rs45502703(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position2057112
GeneTSC2
is asnp
is mentioned by
dbSNPrs45502703
ebirs45502703
HLIrs45502703
Exacrs45502703
Varsomers45502703
Maprs45502703
PheGenIrs45502703
hapmaprs45502703
1000 genomesrs45502703
hgdprs45502703
ensemblrs45502703
gopubmedrs45502703
geneviewrs45502703
scholarrs45502703
googlers45502703
pharmgkbrs45502703
gwascentralrs45502703
openSNPrs45502703
23andMers45502703
23andMe allrs45502703
SNP Nexus

SNPshotrs45502703
SNPdbers45502703
MSV3drs45502703
GWAS Ctlgrs45502703
Max Magnitude0
GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele G
P-val 5E-6
Odds Ratio .03 [NR] ng/mL increase


ClinVar
Risk rs45502703(C;C)
Alt rs45502703(C;C)
Reference rs45502703(G;G)
Significance Untested
Disease not specified Tuberous sclerosis syndrome
Variation info
Gene TSC2
CLNDBN not specified Tuberous sclerosis syndrome
Reversed 0
HGVS NC_000016.9:g.2107113G>A; NC_000016.9:g.2107113G>C
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000190055.2, RCV000042647.2,